Homo sapiens (human): 54556
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Entry
54556 CDS
T01001
Symbol
ING3, Eaf4, ING2, MEAF4, p47ING3
Name
(RefSeq) inhibitor of growth family member 3
KO
K11319
inhibitor of growth protein 3
Organism
hsa
Homo sapiens (human)
Pathway
hsa03082
ATP-dependent chromatin remodeling
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09120 Genetic Information Processing
09126 Chromosome
03082 ATP-dependent chromatin remodeling
54556 (ING3)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03036 Chromosome and associated proteins [BR:
hsa03036
]
54556 (ING3)
Chromosome and associated proteins [BR:
hsa03036
]
Eukaryotic type
Histone modification proteins
HAT complexes
TIP60 complex
54556 (ING3)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
ING
PHD
TorS_sensor_domain
zf-HC5HC2H
Pet100
Suv3_C_1
Motif
Other DBs
NCBI-GeneID:
54556
NCBI-ProteinID:
NP_061944
OMIM:
607493
HGNC:
14587
Ensembl:
ENSG00000071243
UniProt:
Q9NXR8
Structure
PDB
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All DBs
Position
7:120950777..120977216
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AA seq
418 aa
AA seq
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MLYLEDYLEMIEQLPMDLRDRFTEMREMDLQVQNAMDQLEQRVSEFFMNAKKNKPEWREE
QMASIKKDYYKALEDADEKVQLANQIYDLVDRHLRKLDQELAKFKMELEADNAGITEILE
RRSLELDTPSQPVNNHHAHSHTPVEKRKYNPTSHHTTTDHIPEKKFKSEALLSTLTSDAS
KENTLGCRNNNSTASSNNAYNVNSSQPLGSYNIGSLSSGTGAGAITMAAAQAVQATAQMK
EGRRTSSLKASYEAFKNNDFQLGKEFSMARETVGYSSSSALMTTLTQNASSSAADSRSGR
KSKNNNKSSSQQSSSSSSSSSLSSCSSSSTVVQEISQQTTVVPESDSNSQVDWTYDPNEP
RYCICNQVSYGEMVGCDNQDCPIEWFHYGCVGLTEAPKGKWYCPQCTAAMKRRGSRHK
NT seq
1257 nt
NT seq
+upstream
nt +downstream
nt
atgttgtacctagaagactatctggaaatgattgagcagcttcctatggatctgcgggac
cgcttcacggaaatgcgcgagatggacctgcaggtgcagaatgcaatggatcaactagaa
caaagagtcagtgaattctttatgaatgcaaagaaaaataaacctgagtggagggaagag
caaatggcatccatcaaaaaagactactataaagctttggaagatgcagatgagaaggtt
cagttggcaaaccagatatatgacttggtagatcgacacttgagaaagctggatcaggaa
ctggctaagtttaaaatggagctggaagctgataatgctggaattacagaaatattagag
aggcgatctttggaattagacactccttcacagccagtgaacaatcaccatgctcattca
catactccagtggaaaaaaggaaatataatccaacttctcaccatacgacaacagatcat
attcctgaaaagaaatttaaatctgaagctcttctatccacccttacgtcagatgcctct
aaggaaaatacactaggttgtcgaaataataattccacagcctcttctaacaatgcctac
aatgtgaattcctcccaacctctgggatcctataacattggctcgttatcttcaggaact
ggtgcaggggcaattaccatggcagctgctcaagcagttcaggctacagctcagatgaag
gagggacgaagaacatcaagtttaaaagccagttatgaagcatttaagaataatgacttt
cagttgggaaaagaattttcaatggccagggaaacagttggctattcatcatcttcggca
cttatgacaacattaacacagaatgccagttcatcagcagccgactcacggagtggtcga
aagagcaaaaacaacaacaagtcttcaagccagcagtcatcatcttcctcctcctcttct
tccttatcatcgtgttcttcatcatcaactgttgtacaagaaatctctcaacaaacaact
gtagtgccagaatctgattcaaatagtcaggttgattggacttacgacccaaatgaacct
cgatactgcatttgtaatcaggtatcttatggtgagatggtgggatgtgataaccaagat
tgccctatagaatggttccattatggctgcgttggattgacagaggcaccaaaaggcaaa
tggtactgtccacagtgcactgctgcaatgaagagaagaggcagcagacacaaataa
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